NDC 72338-200
Bortezomib 3.5 mg injection, powder, lyophilized, for solution
On the label: Waverley Pharma Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Reliance Life Sciences Private Limited | Navi Mumbai, India | Makes it, makes the active ingredient and packages it | Serious problems, FDA actionFeb 27, 2026 · 8 inspections, 2 with FDA action |
Product details
- Generic drug
- Bortezomib: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous; subcutaneous
- Strength
- 3.5 mg
- Approval
- ANDA ANDA211898
- On the market since
- Jun 19, 2018
- Package NDCs
72338-200-01- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2022
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